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Indian Army Sterile Hypodermic Syringes Tender 2026 IS 10258 IS 550 MDR ISO 9001

Bid Publish Date

10-Jun-2026, 8:02 am

Bid End Date

20-Jun-2026, 9:00 am

Location

JALANDHAR , PUNJAB

Progress

Issue10-Jun-2026, 8:02 am
AwardPending
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Quantity

1380

Category

Single Use Sterile Hypodermic Syringes for Human Use Conforming to IS 10258 (Part 1)

Bid Type

Two Packet Bid

Categories 2

Tender Overview

The Indian Army, Department of Military Affairs, invites bids for Single Use Sterile Hypodermic Syringes for Human Use conforming to IS 10258 (Part 1) (Q2). Bids target suppliers with 3 years govt/PSU supply experience, ISO 9001, and OEM authorization. Key terms include 50% quantity option, and mandatory documents (PAN, GST, EFT mandate). The procurement emphasizes compliance with Drugs and Cosmetic Act 1940 and MDR 2017, with an emphasis on after-sales support for imported products via an Indian registered office. Location context reflects nationwide Indian Army requirements, with emphasis on medical device licensing and material testing.

A unique differentiator is the requirement for Medical Device license validity and BIS/type certification, ensuring product safety. The tender presents a structured path for vendors to demonstrate reliability, supply capacity, and compliance with regulatory standards, while allowing optional quantity adjustments during contract execution.

Technical Specifications & Requirements

  • Product category: Single Use Sterile Hypodermic Syringes for human use; needle included
  • Nominal capacity: per BOQ (ml) with must-have needle integration
  • Packaging: packs with specified pieces per pack
  • Certifications: compliance with Drugs and Cosmetic Act 1940 and MDR 2017; valid Medical Device license issued by competent authority; ISO 9001 certification for bidder or OEM
  • Quality controls: Material Test Certificate required; buyer lab testing governs acceptance; BIS/type test certificates and OEM authorizations to be uploaded
  • OEM/import considerations: Imported products require an Indian registered office for after-sales service; primary supplier must provide manufacturer authorization
  • Delivery/quantity flexibility: Optional clause permits up to 50% up/down quantity variation with proportional delivery adjustments; delivery timelines align to contract terms
  • Documentation: PAN, GST, cancelled cheque, EFT mandate; vendor code creation prerequisites; contractor must provide supplier contracts demonstrating annual quantity across years
  • Special requirements: All products must meet IS 10258 (Part 1) Q2 standards; ongoing supplier certifications to be maintained

Terms, Conditions & Eligibility

  • EMD/Performance: Ensure eligibility with required bid security as per ATC; qualify by meeting 3 years of government/PSU supply experience with relevant contracts
  • Experience & OEM: OEM authorization mandatory if bidding through resellers; primary product must meet the highest-value criterion in bunch bids
  • Documentation: Attach PAN, GSTIN, cancelled cheque; EFT mandate certified by bank; BIS/license/type test certificates and other compliance documents
  • ISO & Testing: ISO 9001 certified bidder or OEM; Material Test Certificate to accompany supply; supplier must pass buyer’s lab tests for acceptance
  • Delivery & Payment: Flexible delivery window with option clause; ensure adherence to any extended delivery periods and contract delivery schedules
  • Warranty/Support: After-sales service obligations for imported products; ensure Indian office for service support; ensure license validity under MDR 2017

Key Specifications

    • Needle included with each syringe
    • Nominal capacity as specified for each pack (ml)
    • Number of pieces in a pack must be as per packaging requirements
    • Compliance with Drugs and Cosmetic Act 1940 and MDR 2017
    • Valid Medical Device license issued by competent authority
    • ISO 9001 certification for bidder or OEM
    • Material Test Certificate to accompany supply
    • OEM authorization for authorized distributors/suppliers
    • For imported products: registered Indian office for after-sales service

Terms & Conditions

  • EMD as per tender; documentation to prove bid security and party eligibility

  • 3 years of govt/PSU supply experience with relevant contracts

  • 50% quantity variation right and extended delivery period terms

  • OEM authorization and Indian service presence for imported items

  • ISO 9001, Medical Device license, and IS/ MDR compliance

  • Material Test Certificate and lab-based acceptance criteria

Important Clauses

Payment Terms

Details not specified; bidders should monitor ATC for payment terms and any advance vs. milestone payments.

Delivery Schedule

Option clause allows up to 50% quantity variation with corresponding delivery adjustments; delivery period linked to last delivery order date.

Penalties/Liquidated Damages

Penalties or LD clauses are likely per standard procurement terms; ensure compliance with delivery timelines to avoid LD.

Bidder Eligibility

  • 3 years or more of regular supply of similar syringes to Central/State Govt or PSUs

  • ISO 9001 certification (bidder or OEM)

  • OEM authorization if bidding through distributors

  • Medical Device license validity for the product

  • Material Test Certificate and BIS/type test certificates as applicable

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Single Use Sterile Hypodermic Syringes for Human Use Conforming to IS 10258 (Part 1) (Q2)

Authority Records

MINISTRY OF DEFENCEMILITARY AFFAIRS DEPARTMENT

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Bid Preparation GeM Registration Document Filing

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Documents 7

GeM-Bidding-9375275.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

CATALOG-Specification-2

CATALOG Specification

Other Documents

OTHER

Other Documents

OTHER

Buyer uploaded ATC document

ATC

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Technical Specifications 2 Items

Item #1 Details

View Catalog
Category Specification Requirement
PRODUCT INFORMATION Needle included Yes
PRODUCT INFORMATION Nominal Capacity of Syringe (ml) ≥ 50
PACKAGING Number of pieces in a Pack 50
CERTIFICATIONS Compliance to Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS Availability of valid Medical Device license for the product issued from the competent authority Yes

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Historical Data

Required Documents

1

Copy of PAN Card

2

Copy of GSTIN

3

Copy of Cancelled Cheque

4

Copy of EFT Mandate certified by Bank

5

Proof of 3 years govt/PSU supply of same/similar syringes with contract copies

6

Manufacturer Authorization / OEM certificate

7

ISO 9001 certification (bidder or OEM)

8

Medical Device license for the product

9

Material Test Certificate

10

BIS license and type test certificates (if applicable)

Frequently Asked Questions

How to bid for Indian Army sterile syringe tender 2026 in India

Bidders must meet 3-year govt/PSU supply experience, upload PAN, GSTIN, EFT mandate, and cancelled cheque. Ensure Medical Device license validity, ISO 9001 certification, and OEM authorization. Include Material Test Certificates and BIS/type test certificates. Submission of relevant contract copies strengthens eligibility and chance of award.

What documents are required for syringe procurement tender in India

Required docs include PAN, GSTIN, cancelled cheque, EFT mandate, OEM authorization if applicable, ISO 9001 certificate, Medical Device license, Material Test Certificate, and government/PSU supply contracts proving 3-year experience. Additional BIS/type test certifications may be requested by the buyer.

What standards apply to single use sterile syringes for human use

Standards include IS 10258 (Part 1) Q2, Drugs and Cosmetic Act 1940 with MDR 2017 amendments, and Medical Device licensing. Suppliers must ensure ISI/BIS compliance where applicable and ISO 9001 certification for the manufacturing process.

When is delivery flexibility allowed for syringe orders in this tender

The purchase allows an option clause enabling up to 50% quantity fluctuation at contract placement and during currency, with delivery time adjusted proportionally to the added quantity, subject to a minimum 30 days minimum extension.

What are the key eligibility criteria for bidders supplying syringes

Eligibility includes 3 years of govt/PSU supply of similar products, OEM authorization, ISO 9001 certification, Medical Device license validity, and ability to provide Material Test Certificate. Demonstrate past contracts with quantity totals to meet annual benchmarks.

What is required for imported syringe products under this tender

Imported items must have an Indian registered office for after-sales service; provide OEM/authorized seller certificates, and ensure local service support capability. The bidder should demonstrate warranty terms and availability of service centers in India.

What certificates should accompany the bid for syringe supply

Submit Medical Device license, ISO 9001 certificate, BIS/type test certificates, and Material Test Certificate. Provide OEM authorization, and proof of government/PSU contracts demonstrating three-year supply experience to strengthen the bid.

How to demonstrate 3 years govt procurement experience for syringes

Provide copies of relevant contracts with Central/State Govt or PSUs, showing quantity shipped per year and the contracting agency. If proposing a bunch bid, ensure the primary product value meets the criterion and attach supporting purchase orders.

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